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Merck

SML0435

Sigma-Aldrich

AF-DX 116

≥98% (HPLC)

别名:

11-[[2-[(二乙胺基)甲基]-1-哌啶基]乙酰基]-5,1 1-二氢-6-吡啶并[2,3-b][1,4]苯二氮卓-6-酮, Otenzepad

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About This Item

经验公式(希尔记法):
C24H31N5O2
分子量:
421.54
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.77

化驗

≥98% (HPLC)

形狀

powder

藥物控制

regulated under CDSA - not available from Sigma-Aldrich Canada

顏色

white to beige

溶解度

DMSO: 5 mg/mL (clear solution; warmed)

儲存溫度

room temp

SMILES 字串

CCN(CC)CC1CCCCN1CC(=O)N2c3ccccc3C(=O)Nc4cccnc24

InChI

1S/C24H31N5O2/c1-3-27(4-2)16-18-10-7-8-15-28(18)17-22(30)29-21-13-6-5-11-19(21)24(31)26-20-12-9-14-25-23(20)29/h5-6,9,11-14,18H,3-4,7-8,10,15-17H2,1-2H3,(H,26,31)

InChI 密鑰

UBRKDAVQCKZSPO-UHFFFAOYSA-N

應用

AF-DX 116 用作 M2 毒蕈碱受体(M2AChR)选择性拮抗剂,以研究 M2AChR 对年轻糖尿病大鼠齿状回基底和碳水化合物刺激长期增强(DG-LTP)的调节和海马细胞前神经生长因子(proNGF)分泌的影响。

生化/生理作用

AF-DX 116 可在反复冷应激诱导的低血压大鼠模型中升高血压和心率。因此,它可以治疗与迷走神经症型自主神经功能障碍相关的低血压。
AF-DX 116是一种选择性M2毒蕈碱乙酰胆碱受体拮抗剂。

特點和優勢

该化合物在受体分类和信号转导手册的 乙酰胆碱受体(毒蕈碱) 页面上有详细描述。想要浏览手册的其他页面, 请单击此处

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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This study was designed to investigate the effects of the cholinesterase inhibitors soman and pyridostigmine bromide (PB) on synaptic transmission in the CA1 field of rat hippocampal slices. Soman (1-100 nM, 10-15 min) decreased the amplitude of GABAergic postsynaptic currents
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American journal of veterinary research, 68(3), 313-322 (2007-03-03)
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European journal of pharmacology, 492(2-3), 183-187 (2004-06-05)
The effects of anticholinergic drugs selective for muscarinic receptor subtypes on prepulse inhibition of acoustic startle response were determined in mice. The prepulse inhibition is associated with sensorimotor information processing in the brain. The anticholinergic agent scopolamine (0.3 mg/kg, s.c.)
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Neurobiology of learning and memory, 79(2), 184-193 (2003-02-20)
A number of studies have implicated cholinergic activity in the mediation of learning and memory processes. However, the specific role of muscarinic receptors in memory formation mechanisms is less known. The aim of the present study is to evaluate the

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